From silicone gel bleed chemistry to skeletal muscle and lipid alterations: clinical and in vitro evidence

Couturier, N.; Randrianaridera, E.; Le, C.; Mutlu, H.; Pluvy, I.; Monnien, F.; Bibeau, F.; anselme, k.; Ponche, A.; Brigaud, I.

doi:10.64898/2026.08.22.746421

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bioRxiv · 10.64898/2026.08.22.746421

From silicone gel bleed chemistry to skeletal muscle and lipid alterations: clinical and in vitro evidence

Couturier, N.·Randrianaridera, E.·Le, C.·Mutlu, H.·Pluvy, I.·Monnien, F.·Bibeau, F.·anselme, k.·Ponche, A.·Brigaud, I.

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Abstract

Musculoskeletal symptoms are frequently reported following silicone breast implantation. However, the biological mechanisms linking implant-derived silicone exposure to skeletal muscle alterations remain poorly understood, partly because the biological effects of silicone have long been debated in the context of its biocompatibility. Here, we chemically characterized the low-molecular-weight fraction of the breast implant silicone exposome, readily released from implant gel through gel bleed, and investigated its potential biological consequences using an integrated approach combining analytical chemistry, clinical transcriptomics and histology, and controlled in vitro muscle experiments. Transcriptomic analyses of periprosthetic tissues associated with silicone implant rupture revealed unexpected myogenic and neuromuscular signatures in tissue conventionally regarded as predominantly fibrous, together with alterations in lipid metabolism and transport. These findings were supported by histological evidence of close interactions between periprosthetic tissue and skeletal muscle. Chemical analysis of the implant-gel extract detected linear siloxane L2 and cyclic siloxanes D3-D8, with tentative assignment of D9. In vitro, C2C12 cells exposed to the implant-gel extract showed up to 30% reduced viability and decreased expression of key neuromyogenic genes. Together, these findings provide convergent chemical, clinical, and experimental evidence that low-molecular-weight constituents of the breast implant silicone exposome may constitute a biologically active exposure capable of affecting skeletal muscle. The associated alterations in lipid metabolism and transport further provide a mechanistic framework for investigating the cellular handling and potential tissue distribution of hydrophobic silicone-derived species. These findings position silicone gel bleed as a biologically relevant source of chemical exposure rather than solely a material-integrity phenomenon.

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Couturier, N., Randrianaridera, E., Le, C., Mutlu, H., Pluvy, I., Monnien, F., Bibeau, F., anselme, k., Ponche, A., Brigaud, I.. 2026-08-24. From silicone gel bleed chemistry to skeletal muscle and lipid alterations: clinical and in vitro evidence. https://doi.org/10.64898/2026.08.22.746421

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